TY - JOUR
T1 - Approaches to nutritional research using organoids; fructose treatment induces epigenetic changes in liver organoids
AU - Yamazaki, Mirai
AU - Yamada, Hiroya
AU - Munetsuna, Eiji
AU - Ando, Yoshitaka
AU - Mizuno, Genki
AU - Teshigawara, Atsushi
AU - Ichikawa, Hayato
AU - Nouchi, Yuki
AU - Kageyama, Itsuki
AU - Wakasugi, Takuya
AU - Ishikawa, Hiroaki
AU - Ohgami, Nobutaka
AU - Suzuki, Koji
AU - Ohashi, Koji
N1 - Publisher Copyright:
© 2024 Elsevier Inc.
PY - 2024/9
Y1 - 2024/9
N2 - Nutritional researches have successfully used animal models to gain new insights into nutrient action. However, comprehensive descriptions of their molecular mechanisms of action remain elusive as appropriate in vitro evaluation systems are lacking. Organoid models can mimic physiological structures and reproduce in vivo functions, making them increasingly utilized in biomedical research for a better understand physiological and pathological phenomena. Therefore, organoid modeling can be a powerful approach for to understand the molecular mechanisms of nutrient action. The present study aims to demonstrate the utility of organoids in nutritional research by further investigating the molecular mechanisms responsible for the negative effects of fructose intake using liver organoids. Here, we treated liver organoids with fructose and analyzed their gene expression profiles and DNA methylation levels. Microarray analysis demonstrated that fructose-treated organoids exhibited increased selenoprotein p (Sepp1) gene expression, whereas pyrosequencing assays revealed reduced DNA methylation levels in the Sepp1 region. These results were consistent with observations using hepatic tissues from fructose-fed rats. Conversely, no differences in Sepp1 mRNA and DNA methylation levels were observed in two-dimensional cells. These results suggest that organoids serve as an ideal in vitro model to recapitulate in vivo tissue responses and help to validate the molecular mechanisms of nutrient action compared to conventional cellular models.
AB - Nutritional researches have successfully used animal models to gain new insights into nutrient action. However, comprehensive descriptions of their molecular mechanisms of action remain elusive as appropriate in vitro evaluation systems are lacking. Organoid models can mimic physiological structures and reproduce in vivo functions, making them increasingly utilized in biomedical research for a better understand physiological and pathological phenomena. Therefore, organoid modeling can be a powerful approach for to understand the molecular mechanisms of nutrient action. The present study aims to demonstrate the utility of organoids in nutritional research by further investigating the molecular mechanisms responsible for the negative effects of fructose intake using liver organoids. Here, we treated liver organoids with fructose and analyzed their gene expression profiles and DNA methylation levels. Microarray analysis demonstrated that fructose-treated organoids exhibited increased selenoprotein p (Sepp1) gene expression, whereas pyrosequencing assays revealed reduced DNA methylation levels in the Sepp1 region. These results were consistent with observations using hepatic tissues from fructose-fed rats. Conversely, no differences in Sepp1 mRNA and DNA methylation levels were observed in two-dimensional cells. These results suggest that organoids serve as an ideal in vitro model to recapitulate in vivo tissue responses and help to validate the molecular mechanisms of nutrient action compared to conventional cellular models.
KW - Epigenetics
KW - Food
KW - Hepatocyte
KW - Nonalcoholic fatty liver disease
KW - Nutrients
KW - Organoid
UR - http://www.scopus.com/inward/record.url?scp=85195195135&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85195195135&partnerID=8YFLogxK
U2 - 10.1016/j.jnutbio.2024.109671
DO - 10.1016/j.jnutbio.2024.109671
M3 - Article
C2 - 38768870
AN - SCOPUS:85195195135
SN - 0955-2863
VL - 131
JO - Journal of Nutritional Biochemistry
JF - Journal of Nutritional Biochemistry
M1 - 109671
ER -